PEDICRAFT, INC.

FDA Device Registration & Listing · JACKSONVILLE, FL, US · Registration 1043568

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
1043568
FEI Number
1043568
Entity Name
PEDICRAFT, INC.
City/State/Country
JACKSONVILLE, FL, US
Establishment Address
4134 ST. AUGUSTINE RD., P.O. BOX 5969, JACKSONVILLE, FL 32247, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
PEDICRAFT, INC. (Owner Number: 1043568)
Owner / Operator Contact Address
4134 ST. AUGUSTINE RD., P.O. BOX 5969, Jacksonville, FL 32247, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Stay Safe Bed Canopy Enclosed Bed PEDICRAFT INFANT CRIB PEDICRAFT NEONATAL CRIB PEDICRAFT HOMECARE CRIB PEDICRAFT HOSPITAL CRIB u-design Bassinet Pedicraft Bassinet

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FNJ Bed, Manual General Hospital Class 1 880.5120 1992-07-21
FMS Bed, Pediatric Open Hospital General Hospital Class 2 880.5140 2002-04-04
NZG Bassinet, Hospital General Hospital Class 2 880.5145 2015-05-07

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PEDICRAFT, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1043568. Last updated year: 2026. Please use registration number 1043568 when referencing this establishment in official correspondence.
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